International trends in the uptake of cancer risk reduction strategies in women with a BRCA1 or BRCA2 mutation.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
07 2019
Historique:
received: 31 07 2018
accepted: 19 03 2019
revised: 15 03 2019
pubmed: 12 4 2019
medline: 11 3 2020
entrez: 12 4 2019
Statut: ppublish

Résumé

Women with a BRCA1 or BRCA2 mutation face high risks of breast and ovarian cancer. In the current study, we report on uptake of cancer screening and risk-reduction options in a cohort of BRCA mutation carriers from ten countries over two time periods (1995 to 2008 and 2009 to 2017). Eligible subjects were identified from an international database of female BRCA mutation carriers and included women from 59 centres from ten countries. Subjects completed a questionnaire at the time of genetic testing, which included past use of cancer prevention options and screening tests. Biennial follow-up questionnaires were administered. Six-thousand two-hundred and twenty-three women were followed for a mean of 7.5 years. The mean age at last follow-up was 52.1 years (27-96 years) and 42.3% of the women had a prior diagnosis of breast cancer. In all, 27.8% had a prophylactic bilateral mastectomy and  64.7% had a BSO. Screening with breast MRI increased from 70% before 2009 to 81% at or after 2009. There were significant differences in uptake of all options by country. For women who received genetic testing more recently, uptake of prophylactic mastectomy and breast MRI is significantly higher than those who received genetic testing more than 10 years ago. However, uptake of both BSO and breast MRI is not optimal, and interventions to increase uptake are needed.

Sections du résumé

BACKGROUND
Women with a BRCA1 or BRCA2 mutation face high risks of breast and ovarian cancer. In the current study, we report on uptake of cancer screening and risk-reduction options in a cohort of BRCA mutation carriers from ten countries over two time periods (1995 to 2008 and 2009 to 2017).
METHODS
Eligible subjects were identified from an international database of female BRCA mutation carriers and included women from 59 centres from ten countries. Subjects completed a questionnaire at the time of genetic testing, which included past use of cancer prevention options and screening tests. Biennial follow-up questionnaires were administered.
RESULTS
Six-thousand two-hundred and twenty-three women were followed for a mean of 7.5 years. The mean age at last follow-up was 52.1 years (27-96 years) and 42.3% of the women had a prior diagnosis of breast cancer. In all, 27.8% had a prophylactic bilateral mastectomy and  64.7% had a BSO. Screening with breast MRI increased from 70% before 2009 to 81% at or after 2009. There were significant differences in uptake of all options by country.
CONCLUSION
For women who received genetic testing more recently, uptake of prophylactic mastectomy and breast MRI is significantly higher than those who received genetic testing more than 10 years ago. However, uptake of both BSO and breast MRI is not optimal, and interventions to increase uptake are needed.

Identifiants

pubmed: 30971774
doi: 10.1038/s41416-019-0446-1
pii: 10.1038/s41416-019-0446-1
pmc: PMC6738089
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

15-21

Commentaires et corrections

Type : CommentIn

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Auteurs

Kelly Metcalfe (K)

Women's College Research Institute, Toronto, ON, Canada.
Bloomberg, Faculty of Nursing, University of Toronto, Toronto, ON, Canada.

Andrea Eisen (A)

Toronto-Sunnybrook Regional Cancer Center, Toronto, ON, Canada.

Leigha Senter (L)

Division of Human Genetics, The Ohio State University Medical Center, Comprehensive Cancer Center, Columbus, OH, USA.

Susan Armel (S)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Toronto, Toronto, ON, Canada.

Louise Bordeleau (L)

Juravinksi Cancer Centre, Hamilton, ON, L8V 5C2, Canada.

Wendy S Meschino (WS)

North York General Hospital, Toronto, ON, Canada.

Tuya Pal (T)

Vanderbilt-Ingram Cancer Center/Vanderbilt University Medical Center, Nashville, TN, USA.

Henry T Lynch (HT)

Hereditary Cancer Center, Creighton University School of Medicine, Omaha, NE, USA.

Nadine M Tung (NM)

Beth Israel Deaconess Medical Center, Boston, MA, USA.

Ava Kwong (A)

Department of Surgery, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong SAR.
Department of Surgery, Hong Kong Sanatorium & Hospital, Happy Valley, Hong Kong SAR.
Hong Kong Hereditary Breast Cancer Family Registry, Happy Valley, Hong Kong SAR.

Peter Ainsworth (P)

Department of Population Sciences, Beckman Research Institute of City of Hope, Duarte, CA, USA.

Beth Karlan (B)

Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, West Hollywood, CA, USA.

Pal Moller (P)

Research Group Inherited Cancer, Department of Medical, Genetics, Oslo University Hospital, Oslo, Norway.
Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, part of Oslo University Hospital, Oslo, Norway.
Center for Hereditary Tumors, HELIOS-Klinikum Wuppertal, University of Witten-Herdecke, Wuppertal, Germany.

Charis Eng (C)

Genomic Medicine Institute, Center for Personalised Genetic Healthcare, Cleveland Clinic, Cleveland, OH, USA.

Jeffrey N Weitzel (JN)

City of Hope National Medical Center, Duarte, CA, USA.

Ping Sun (P)

Women's College Research Institute, Toronto, ON, Canada.

Jan Lubinski (J)

International Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Steven A Narod (SA)

Women's College Research Institute, Toronto, ON, Canada. steven.narod@wchospital.ca.
Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada. steven.narod@wchospital.ca.

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